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Rhes Suppression Enhances Disease Phenotypes in Huntington’s Disease Mice

In Huntington’s disease (HD) mutant HTT is ubiquitously expressed yet the striatum undergoes profound early degeneration. Cell culture studies suggest that a striatal-enriched protein, Rhes, may account for this vulnerability. We investigated the therapeutic potential of silencing Rhes in vivo using...

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Hlavní autoři: Lee, John H., Sowada, Matthew J., Boudreau, Ryan L., Aerts, Andrea M., Thedens, Daniel R., Nopoulos, Peg, Davidson, Beverly L.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2014
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4139702/
https://ncbi.nlm.nih.gov/pubmed/25062765
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JHD-140094
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